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Motor disability
Motor disturbance
Nerval impairment of motion
Nerval incoordination of movements
Nerval motor disturbance
Psychogenic impairment of motion
Psychogenic incoordination of movements
Psychogenic motor disturbance
Pyramidal incoordination of movements
Pyramidal motor disturbance
Pyramidal syndrome
Upper motor neuron lesion

Traduction de «pyramidal motor disturbance » (Anglais → Français) :

pyramidal incoordination of movements | pyramidal motor disturbance
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
syndrome pyramidal | trouble moteur pyramidal
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
motor disturbance | motor disability
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
trouble moteur
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
nerval impairment of motion | nerval incoordination of movements | nerval motor disturbance
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
trouble moteur neurogène
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
psychogenic impairment of motion | psychogenic incoordination of movements | psychogenic motor disturbance
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
trouble moteur psychogène
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Main features described as slowly progressive cerebellar syndrome and epilepsy, sometimes mild pyramidal signs, peripheral neuropathy and neuropsychological disturbances. Prevalence is unknown. Many kindreds have been found in Mexican and Brazilian p
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
ataxie spinocérébelleuse type 10
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
A rare hereditary ataxia with characteristics of delayed early motor development, severe neonatal hypotonia, non-progressive ataxia and slow eye movements, presenting normal cognitive abilities and absence of pyramidal signs. Frequently patients also
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
ataxie cérébelleuse liée à l'X non progressive
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
A rare epilepsy syndrome with characteristics of recurrent, long-lasting myoclonic status in infants and young children with a non-progressive encephalopathy, associated with transient and recurring motor, cognitive and/or behavioral disturbances.
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
epilepsie myoclonique des encéphalopathies non-progressives
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
pyramidal syndrome | upper motor neuron lesion
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
syndrome pyramidal
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]


D'autres ont cherché : motor disability     motor disturbance     nerval impairment of motion     nerval incoordination of movements     nerval motor disturbance     psychogenic impairment of motion     psychogenic incoordination of movements     psychogenic motor disturbance     pyramidal incoordination of movements     pyramidal motor disturbance     pyramidal syndrome     upper motor neuron lesion     


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Date index: 2021-03-05
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